eudamed_udi
Primary ID: 28053326000045
eSwab (UDI 28053326000045)
Manufactured by Copan Italia S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for eSwab - Primary ID 28053326000045
Device Regulatory Overview
The eSwab (Model/Catalog Number: 480CESR) is a medical device manufactured by Copan Italia S.P.A.. This product is indexed under FDA Product Code / Category Classification A1102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 480CESR
- Product Code / EMDN
- A1102
- Device Name
- ESWAB LQ AMIES REG. FLOCK DOUBLE WRAPPED
- Database Sync Date
- 2026-08-09 16:29:58
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of eSwab?
The registered manufacturer of record for eSwab is Copan Italia S.P.A..
What is the Primary UDI-DI identifier for eSwab?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 28053326000045.
What classification code is assigned to this device?
This device is registered under product classification code A1102.
Similar Classification Devices (A1102)
Other Devices by Copan Italia S.P.A.
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